A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996944



Internal ID65488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63652389..63845779hg38UCSC Ensembl
chr7:63112767..63306157hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38193391
hg19193391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996944
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003281


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